Iodine-Catalyzed Synthesis of Highly Functionalized 1,4-Dihydropyridines from 2-Aminobenzothiazole, Aryl Aldehydes and Meldrum’s Acid via Diels-Alder [4 + 2] Cycloaddition Reaction-Reference-Cited by-同舟云学术

Iodine-Catalyzed Synthesis of Highly Functionalized 1,4-Dihydropyridines from 2-Aminobenzothiazole, Aryl Aldehydes and Meldrum’s Acid via Diels-Alder [4 + 2] Cycloaddition Reaction

Published:2021-10-19 Issue: Volume: Page:1-8
ISSN:1040-6638
Container-title:Polycyclic Aromatic Compounds
language:en
Short-container-title:Polycyclic Aromatic Compounds

Author:

Mehrabi Hossein¹,Najafian-Ashrafi Faezeh¹

Affiliation:

1. Department of Chemistry, Vali-e-Asr University of Rafsanjan, Rafsanjan, Iran

Publisher

Informa UK Limited

Subject

Materials Chemistry,Organic Chemistry,Polymers and Plastics

Link

https://www.tandfonline.com/doi/pdf/10.1080/10406638.2021.1991398

Reference25 articles.

1. Synthesis and biological evaluation of N-aryl-1,4-dihydropyridines as novel antidyslipidemic and antioxidant agents

2. Synthesis and biological evaluation of some new 1,4-dihydropyridines containing different ester substitute and diethyl carbamoyl group as anti-tubercular agents

3. 3,5-Dibenzoyl-1,4-dihydropyridines: Synthesis and MDR Reversal in Tumor Cells

4. L-type Ca2+ channel modulation by dihydropyridines potentiates κ-opioid receptor agonist induced acute analgesia and inhibits development of tolerance in rats

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